The Medial Temporal Lobe and Recognition Memory

The Cognitive neurosciences

(2005) · Choice Reviews Online · doi:10.5860/choice.43-0626 · Cited by 4,726

The Nature of Recollection and Familiarity: A Review of 30 Years of Research

Yonelinas, A. P. (2002) · Journal of Memory and Language · doi:10.1006/jmla.2002.2864 · Cited by 3,840

A process dissociation framework: Separating automatic from intentional uses of memory

Jacoby, L. L. (1991) · Journal of Memory and Language · doi:10.1016/0749-596x(91)90025-f · Cited by 3,817

Object vision and spatial vision: Two cortical pathways

Mishkin, M., Ungerleider, L. G., & Macko, K. A. (1983) · Trends in Neurosciences · doi:10.1016/0166-2236(83)90190-x · Cited by 2,947

Repetition and the brain: neural models of stimulus-specific effects

Grill-Spector, K., Henson, R., & Martin, A. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.11.006 · Cited by 2,256

Hippocampus, space, and memory

Olton, D. S., Becker, J. T., & Handelmann, G. E. (1979) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00062713 · Cited by 2,018

Human amnesia and the medial temporal region: enduring memory impairment following a bilateral lesion limited to field CA1 of the hippocampus

Zola-Morgan, S., Squire, L., & Amaral, D. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-10-02950.1986 · Cited by 1,997

How many memory systems are there?

Tulving, E. (1985) · American Psychologist · doi:10.1037/0003-066x.40.4.385 · Cited by 1,909

Episodic memory, amnesia, and the hippocampal–anterior thalamic axis

Aggleton, J. P., & Brown, M. W. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99002034 · Cited by 1,879

Differential Effects of Early Hippocampal Pathology on Episodic and Semantic Memory

Vargha-Khadem, F., Gadian, D. G., Watkins, K. E., Connelly, A., Van Paesschen, W., & Mishkin, M. (1997) · Science · doi:10.1126/science.277.5324.376 · Cited by 1,746

Longitudinal imaging pattern analysis (SPARE-CD index) detects early structural and functional changes before cognitive decline in healthy older adults

Clark, V. H., Resnick, S. M., Doshi, J. J., Beason‐Held, L. L., Zhou, Y., Ferrucci, L., Wong, D. F., Kraut, M. A., & Davatzikos, C. A. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.01.010 · Cited by 39

Working memory decline in normal aging: Memory load and representational demands affect performance

Klencklen, G., Lavenex, P. B., Brandner, C., & Lavenex, P. (2017) · Learning and Motivation · doi:10.1016/j.lmot.2017.09.002 · Cited by 38

The contribution of different prefrontal cortex regions to recollection and familiarity: a review of fMRI data

Scalici, F., Caltagirone, C., & Carlesimo, G. A. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.10.017 · Cited by 41

Differential role of interleukin‐1β in neuroinflammation‐induced impairment of spatial and nonspatial memory in hyperammonemic rats

Taoro‐González, L., Cabrera‐Pastor, A., Sancho‐Alonso, M., Arenas, Y. M., Meseguer, F., Balzano, T., Mlili, N. E., & Felipo, V. (2019) · The FASEB Journal · doi:10.1096/fj.201900230rr · Cited by 38

Magnetoencephalography recordings reveal the spatiotemporal dynamics of recognition memory for complex versus simple auditory sequences

Fernández‐Rubio, G., Brattico, E., Kotz, S. A., Kringelbach, M. L., Vuust, P., & Bonetti, L. (2022) · Communications Biology · doi:10.1038/s42003-022-04217-8 · Cited by 38

Domain‐specific retrieval of source information in the medial temporal lobe

Peters, J., Boris Suchan, A., Köster, O., & Daum, I. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05752.x · Cited by 41

The Caudal Medial Entorhinal Cortex: a Selective Role in Recollection-Based Recognition Memory

Sauvage, M. M., Beer, Z., Ekovich, M., Ho, L., & Eichenbaum, H. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4301-10.2010 · Cited by 40

Comparison of neural activity that leads to true memories, false memories, and forgetting: An fMRI study of the misinformation effect

Baym, C. L., & Gonsalves, B. D. (2010) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/cabn.10.3.339 · Cited by 38

Single neuron binding properties and the magical number 7

Migliore, M., Novara, G., & Tegolo, D. (2008) · Hippocampus · doi:10.1002/hipo.20480 · Cited by 39

Familiarity and Conceptual Priming Engage Distinct Cortical Networks

Voss, J. L., Reber, P. J., Mesulam, M. M., Parrish, T. B., & Paller, K. A. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm200 · Cited by 38

Dataset of human medial temporal lobe single neuron activity during declarative memory encoding and recognition

Faraut, M. C. M., Carlson, A. A., Sullivan, S. M., Tudusciuc, O., Ross, I. B., Reed, C. M., Chung, J. M., Mamelak, A. N., & Rutishauser, U. (2018) · Scientific Data · doi:10.1038/sdata.2018.10 · Cited by 41

Hippocampal and prefrontal dopamine D1/5 receptor involvement in the memory-enhancing effect of reboxetine

De Bundel, D., Femenía, T., DuPont, C. M., Konradsson-Geuken, Å., Feltmann, K., Schilström, B., & Lindskog, M. (2013) · International Journal of Neuropsychopharmacology · doi:10.1017/s1461145713000370 · Cited by 37

Types of memory, dementia, Alzheimer’s disease, and their various pathological cascades as targets for potential pharmacological drugs

Akhtar, A., Singh, S., Kaushik, R., Awasthi, R., & Behl, T. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102289 · Cited by 38

Memory-enhancing amygdala stimulation elicits gamma synchrony in the hippocampus.

Bass, D. I., & Manns, J. R. (2015) · Behavioral Neuroscience · doi:10.1037/bne0000052 · Cited by 39

Dissociating the “retrieval success” regions of the brain: Effects of retrieval delay

Huijbers, W., Pennartz, C. M. A., & Daselaar, S. M. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.10.006 · Cited by 37

The effects of developmental alcohol exposure on the neurobiology of spatial processing

Harvey, R. E., Berkowitz, L. E., Hamilton, D. A., & Clark, B. J. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.09.018 · Cited by 40

Hippocampal-medial prefrontal cortex network dynamics predict performance during retrieval in a context-guided object memory task

Morici, J. F., Weisstaub, N., & Zold, C. L. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2203024119 · Cited by 38

Brains of verbal memory specialists show anatomical differences in language, memory and visual systems

Hartzell, J. F., Davis, B., Melcher, D., Miceli, G., Jovicich, J., Nath, T., Singh, N. C., & Hasson, U. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.07.027 · Cited by 38

From the GPS to HM: Place cells, grid cells, and memory

Knierim, J. J. (2015) · Hippocampus · doi:10.1002/hipo.22453 · Cited by 37

Functional cooperation between the hippocampal subregions and the medial septum in unreinforced and reinforced spatial memory tasks

Okada, K., & Okaichi, H. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.02.007 · Cited by 39

Significance of the deep layers of entorhinal cortex for transfer of both perirhinal and amygdala inputs to the hippocampus

Koganezawa, N., Taguchi, A., Tominaga, T., Ohara, S., Tsutsui, K., Witter, M. P., & Iijima, T. (2008) · Neuroscience Research · doi:10.1016/j.neures.2008.02.007 · Cited by 37

Long term follow-up after multiple hippocampal transection (MHT)

Patil, A. A., & Andrews, R. V. (2013) · Seizure · doi:10.1016/j.seizure.2013.05.014 · Cited by 37

Impaired context reversal learning, but not cue reversal learning, in patients with amnestic mild cognitive impairment

Levy‐Gigi, E., Kelemen, O., Gluck, M. A., & Kéri, S. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.08.005 · Cited by 37

Decoding oscillatory representations and mechanisms in memory

Jafarpour, A., Horner, A. J., Fuentemilla, L., Penny, W. D., & Düzel, E. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.04.002 · Cited by 41

Network-based brain stimulation selectively impairs spatial retrieval

Kim, K., Schedlbauer, A. M., Rollo, M. J., Karunakaran, S., Ekstrom, A. D., & Tandon, N. (2017) · Brain stimulation · doi:10.1016/j.brs.2017.09.016 · Cited by 41

Hippocampal hemispheric and long-axis differentiation of stimulus content during episodic memory encoding and retrieval: An activation likelihood estimation meta-analysis

Persson, J., & Söderlund, H. (2015) · Hippocampus · doi:10.1002/hipo.22482 · Cited by 40

Hippocampal–neocortical networks differ during encoding and retrieval of relational memory: Functional and effective connectivity analyses

McCormick, C., Moscovitch, M., Protzner, A. B., Huber, C. G., & McAndrews, M. P. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.07.010 · Cited by 39

Is a novel conceptual unit more than the sum of its parts?: FMRI evidence from an associative recognition memory study

Bader, R., Opitz, B., Reith, W., & Mecklinger, A. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.06.006 · Cited by 36

Old processes, new perspectives: Familiarity is correlated with (not independent of) recollection and is more (not equally) variable for targets than for lures

Moran, R., & Goshen‐Gottstein, Y. (2015) · Cognitive Psychology · doi:10.1016/j.cogpsych.2015.01.005 · Cited by 36

Postnatal development of retrosplenial projections to the parahippocampal region of the rat

Sugar, J., & Witter, M. P. (2016) · eLife · doi:10.7554/elife.13925 · Cited by 36

Implicit memory for words heard during sleep

Andrillon, T., & Kouider, S. (2016) · Neuroscience of Consciousness · doi:10.1093/nc/niw014 · Cited by 37

Consciousness in a multilevel architecture: Evidence from the right side of the brain

Velichkovsky, B. M., Krotkova, O. A., Kotov, A. A., Orlov, V. A., Verkhlyutov, V. M., Ushakov, V., & Sharaev, M. (2018) · Consciousness and Cognition · doi:10.1016/j.concog.2018.06.004 · Cited by 36

Binding deficits in visual short‐term memory in patients with temporal lobe lobectomy

Zokaei, N., Nour, M. M., Sillence, A., Drew, D., Adcock, J., Stacey, R. J., Voets, N., Sen, A., & Husain, M. (2018) · Hippocampus · doi:10.1002/hipo.22998 · Cited by 38

Mental health in familial caregivers of Alzheimer’s disease patients: are the effects of chronic stress on cognition inevitable?

Corrêa, M. S., de Lima, D. B., Giacobbo, B. L., Vedovelli, K., Argimon, I. I. D. L., & Bromberg, E. (2018) · Stress · doi:10.1080/10253890.2018.1510485 · Cited by 40

Postchemotherapy hippocampal functional connectivity patterns in patients with breast cancer: a longitudinal resting state functional MR imaging study

Feng, Y., Tuluhong, D., Shi, Z., Zheng, L. J., Chen, T., Lu, G., Wang, S., & Zhang, L. J. (2019) · Brain Imaging and Behavior · doi:10.1007/s11682-019-00067-x · Cited by 36

Dissociating activation and integration of discourse referents: Evidence from ERPs and oscillations

Coopmans, C. W., & Nieuwland, M. S. (2020) · Cortex · doi:10.1016/j.cortex.2019.12.028 · Cited by 36

Altered connectivity in the right inferior frontal gyrus associated with self-control in adolescents exhibiting problematic smartphone use: A fMRI study

Pyeon, A., Choi, J., Cho, H., Kim, J.-Y., Choi, I. Y., Ahn, K. J., Choi, J., Chun, J., & Kim, D. (2021) · Journal of Behavioral Addictions · doi:10.1556/2006.2021.00085 · Cited by 36

Associations between abstract working memory abilities and brain activity underlying long-term recognition of auditory sequences

Fernández‐Rubio, G., Carlomagno, F., Vuust, P., Kringelbach, M. L., & Bonetti, L. (2022) · PNAS Nexus · doi:10.1093/pnasnexus/pgac216 · Cited by 36

Aberrant Functional Connectivity Architecture in Alzheimer’s Disease and Mild Cognitive Impairment: A Whole-Brain, Data-Driven Analysis

Zhou, B., Yao, H., Wang, P., Zhang, Z., Zhan, Y., Ma, J., Xu, K., Wang, L., An, N., Liu, Y., et al. (2015) · BioMed Research International · doi:10.1155/2015/495375 · Cited by 38

Structural changes in the gray matter of unmedicated patients with obsessive-compulsive disorder: a voxel-based morphometric study

Tan, L., Fan, Q., You, C., Wang, J., Dong, Z., Wang, X., Chen, K., Xiao, Z., & Jiang, K. (2013) · Neuroscience Bulletin · doi:10.1007/s12264-013-1370-7 · Cited by 37

Individual Differences in True and False Memory Retrieval Are Related to White Matter Brain Microstructure

Fuentemilla, L., Càmara, E., Münte, T. F., Krämer, U. M., Toni Cunillera, B., Marco‐Pallarés, J., Tempelmann, C., & Rodríguez‐Fornells, A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5270-08.2009 · Cited by 37

Subjective Experience of Episodic Memory and Metacognition: A Neurodevelopmental Approach

Souchay, C., Guillery‐Girard, B., Pauly‐Takacs, K., Wojcik, D. Z., & Eustache, F. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00212 · Cited by 41

Recollection in adolescents with Autism Spectrum Disorder

Souchay, C., Wojcik, D. Z., Williams, H. L., Crathern, S., & Clarke, P. (2012) · Cortex · doi:10.1016/j.cortex.2012.07.011 · Cited by 36

Dissociable parietal regions facilitate successful retrieval of recently learned and personally familiar information

Elman, J. A., Cohn‐Sheehy, B. I., & Shimamura, A. P. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.12.013 · Cited by 37

When the Brain Decides

Rosburg, T., Mecklinger, A., & Frings, C. (2011) · Psychological Science · doi:10.1177/0956797611417454 · Cited by 36

Memory loss resulting from fornix and septal damage: Impaired supra-span recall but preserved recognition over a 24-hour delay.

Vann, S. D., Denby, C. E., Love, S., Montaldi, D., Renowden, S. A., & Coakham, H. B. (2008) · Neuropsychology · doi:10.1037/a0012542 · Cited by 36

Reorganization of associative memory in humans with long-standing hippocampal damage

Braun, M., Finke, C., Ostendorf, F., Lehmann, T., Hoffmann, K., & Ploner, C. J. (2008) · Brain · doi:10.1093/brain/awn191 · Cited by 36

Perirhinal cortex tracks degree of recent as well as cumulative lifetime experience with object concepts

Duke, D., Martin, C. B., Bowles, B., McRae, K., & Köhler, S. (2017) · Cortex · doi:10.1016/j.cortex.2017.01.015 · Cited by 39

Visual integration enhances associative memory equally for young and older adults without reducing hippocampal encoding activation

Memel, M., & Ryan, L. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.04.031 · Cited by 37

Independent contributions of fMRI familiarity and novelty effects to recognition memory and their stability across the adult lifespan

de Chastelaine, M., Mattson, J. T., Wang, T. H., Donley, B. E., & Rugg, M. D. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.05.039 · Cited by 36

Expected Reward Value and Reward Uncertainty Have Temporally Dissociable Effects on Memory Formation

Stanek, J. K., Dickerson, K. C., Chiew, K. S., Clement, N. J., & Adcock, R. A. (2019) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01411 · Cited by 38

A meta-analysis of event-related potential correlates of recognition memory

Morcom, A., Kwon, S., Rugg, M. D., Curran, T., & Wiegand, R. (2023) · Psychonomic Bulletin & Review · doi:10.3758/s13423-023-02309-y · Cited by 38

Regional-Asymmetric Adaptive Graph Convolutional Neural Network for Diagnosis of Autism in Children With Resting-State EEG

Hu, W., Jiang, G., Han, J., Li, X., & Xie, P. (2023) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2023.3347134 · Cited by 37

Gray and white matter correlates of navigational ability in humans

Wegman, J., Fonteijn, H., van Ekert, J., Tyborowska, A., Jansen, C., & Janzen, G. (2013) · Human Brain Mapping · doi:10.1002/hbm.22349 · Cited by 39

Impact of novelty and type of material on recognition in healthy older adults and persons with mild cognitive impairment

Belleville, S., Ménard, M.-C., & Lepage, É. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.06.011 · Cited by 35

The effects of attention on age-related relational memory deficits: Evidence from a novel attentional manipulation.

Kim, S.-Y., & Giovanello, K. S. (2011) · Psychology and Aging · doi:10.1037/a0022326 · Cited by 38

Higher-Order Conditioning Is Impaired by Hippocampal Lesions

Gilboa, A., Sekeres, M. J., Moscovitch, M., & Winocur, G. (2014) · Current Biology · doi:10.1016/j.cub.2014.07.078 · Cited by 36

Influence of electroencephalography neurofeedback training on episodic memory: A randomized, sham-controlled, double-blind study

Guez, J., Rogel, A., Getter, N., Keha, E., Cohen, T., Amor, T., Gordon, S. C., Meiran, N., & Todder, D. (2014) · Memory · doi:10.1080/09658211.2014.921713 · Cited by 35

Separating Recognition Processes of Declarative Memory via Anodal tDCS: Boosting Old Item Recognition by Temporal and New Item Detection by Parietal Stimulation

Pisoni, A., Turi, Z., Raithel, A. M., Ambrus, G. G., Alekseichuk, I., Schacht, A., Paulus, W., & Antal, A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0123085 · Cited by 37

Memory for items and relationships among items embedded in realistic scenes: Disproportionate relational memory impairments in amnesia.

Hannula, D. E., Tranel, D., Allen, J. S., Kirchhoff, B. A., Nickel, A. E., & Cohen, N. J. (2014) · Neuropsychology · doi:10.1037/neu0000119 · Cited by 36

Impaired assessment of cumulative lifetime familiarity for object concepts after left anterior temporal-lobe resection that includes perirhinal cortex but spares the hippocampus

Bowles, B., Duke, D., Rosenbaum, R. S., McRae, K., & Köhler, S. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.06.035 · Cited by 35

Differential Medial Temporal Lobe and Parietal Cortical Contributions to Real-world Autobiographical Episodic and Autobiographical Semantic Memory

Brown, T. I., Rissman, J., Chow, T. E., Uncapher, M. R., & Wagner, A. D. (2018) · Scientific Reports · doi:10.1038/s41598-018-24549-y · Cited by 38

Neural specificity of scene representations is related to memory performance in childhood

Fandakova, Y., Leckey, S., Driver, C., Bunge, S. A., & Ghetti, S. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.05.050 · Cited by 35

Object and place information processing by CA1 hippocampal neurons of C57BL/6J mice

Ásgeirsdóttir, H. N., Cohen, S. J., & Stackman, R. W. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00278.2019 · Cited by 35

An integrative model of network activity during episodic memory retrieval and a meta-analysis of fMRI studies on source memory retrieval

Kim, H. (2020) · Brain Research · doi:10.1016/j.brainres.2020.147049 · Cited by 35

Age-Related Increases in Posterior Hippocampal Granularity Are Associated with Remote Detailed Episodic Memory in Development

Callaghan, B. L., Gasser, C., Silvers, J. A., VanTieghem, M., Choy, T., O’Sullivan, K., Tompary, A., Davachi, L., & Tottenham, N. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1738-20.2020 · Cited by 41

High resolution structural and functional MRI of the hippocampus in young adults with Down syndrome

Koenig, K. A., Oh, S., Stasko, M. R., Roth, E., Taylor, H. G., Ruedrich, S., Wang, Z. I., Leverenz, J. B., & Costa, A. C. S. (2021) · Brain Communications · doi:10.1093/braincomms/fcab088 · Cited by 38

Dietary strawberry improves cognition in a randomised, double-blind, placebo-controlled trial in older adults

Miller, M. G., Thangthaeng, N., Rutledge, G. A., Scott, T. M., & Shukitt‐Hale, B. (2021) · British Journal Of Nutrition · doi:10.1017/s0007114521000222 · Cited by 35

Eye-movement replay supports episodic remembering

Johansson, R., Nyström, M., Dewhurst, R., & Johansson, M. (2022) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2022.0964 · Cited by 35

Neurocomputational account of memory and perception: Thresholded and graded signals in the hippocampus

Elfman, K. W., Aly, M., & Yonelinas, A. P. (2014) · Hippocampus · doi:10.1002/hipo.22345 · Cited by 35

Sex-dependent behavioral effects of Mthfr deficiency and neonatal GABA potentiation in mice

Levav-Rabkin, T., Blumkin, E., Galron, D., & Golan, H. M. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.08.031 · Cited by 35

Learning and memory in children with Noonan syndrome

Pierpont, E. I., Tworog‐Dube, E., & Roberts, A. E. (2013) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.36075 · Cited by 35

Patterns of brain atrophy associated with episodic memory and semantic fluency decline in aging

Pelletier, A., Bernard, C., Dilharreguy, B., Helmer, C., Goff, M. L., Chanraud, S., Dartigues, J., Michèle Allard, A., Amieva, H., & Catheline, G. (2017) · Aging · doi:10.18632/aging.101186 · Cited by 37

Direct Stimulation of Human Hippocampus During Verbal Associative Encoding Enhances Subsequent Memory Recollection

Jun, S., Kim, J. S., & Chung, C. K. (2019) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2019.00023 · Cited by 39

Effects of Emotional Contexts on Cerebello-Thalamo-Cortical Activity during Action Observation

Mazzola, V., Vuilleumier, P., Latorre, V., Petito, A., Gallese, V., Popolizio, T., Arciero, G., & Bondolfi, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075912 · Cited by 34

Cognitive Decline in Adults with Amnestic Mild Cognitive Impairment and High Amyloid-β: Prodromal Alzheimer's Disease?

Lim, Y. Y., Ellis, K. A., Harrington, K., Pietrzak, R. H., Gale, J., Ames, D. J., Bush, A. I., Darby, D., Martins, R. N., Masters, C. L., et al. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-121771 · Cited by 38

Pain anticipation recruits the mesolimbic system and differentially modulates subsequent recognition memory

Bauch, E. M., Rausch, V. H., & Bunzeck, N. (2014) · Human Brain Mapping · doi:10.1002/hbm.22497 · Cited by 36

Action-Based Learning of Multistate Objects in the Medial Temporal Lobe

Hindy, N. C., & Turk‐Browne, N. B. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv030 · Cited by 34

Hyperactivation of parahippocampal region and fusiform gyrus associated with successful encoding in medial temporal lobe epilepsy

Guedj, É., Bettus, G., Barbeau, E. J., Liégeois‐Chauvel, C., Sylviane Confort-gouny, A., Bartoloméi, F., Chauvel, P., Cozzone, P. J., Ranjeva, J., & Guye, M. (2011) · Epilepsia · doi:10.1111/j.1528-1167.2011.03052.x · Cited by 34

The effect of sleep deprivation on the encoding of contextual and non-contextual aspects of emotional memory

Tempesta, D., Socci, V., Coppo, M., Ioio, G. D., Nepa, V., Gennaro, L. D., & Ferrara, M. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.03.007 · Cited by 34

Memory before and after H.M.: an impressionistic historical perspective

Moscovitch, M. (2012) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780199580286.003.0002 · Cited by 35

Disconnection of the Perirhinal and Postrhinal Cortices Impairs Recognition of Objects in Context But Not Contextual Fear Conditioning

Heimer‐McGinn, V., Poeta, D. L., Aghi, K., Udawatta, M., & Burwell, R. D. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0254-17.2017 · Cited by 34

Dynamic Functional Network Connectivity in Schizophrenia with Magnetoencephalography and Functional Magnetic Resonance Imaging: Do Different Timescales Tell a Different Story?

Sanfratello, L., Houck, J. M., & Calhoun, V. D. (2019) · Brain Connectivity · doi:10.1089/brain.2018.0608 · Cited by 34

Episodic memory contributions to autobiographical memory and open-ended problem-solving specificity in younger and older adults

Peters, S. L., Fan, C. L., & Sheldon, S. (2019) · Memory & Cognition · doi:10.3758/s13421-019-00953-1 · Cited by 34

Task-dependent effects of intracranial hippocampal stimulation on human memory and hippocampal theta power

Jun, S., Lee, S. A., Kim, J. S., Jeong, W., & Chung, C. K. (2020) · Brain stimulation · doi:10.1016/j.brs.2020.01.013 · Cited by 36

Multiple Exposures Enhance Both Item Memory and Contextual Memory Over Time

Chen, H., & Yang, J. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.565169 · Cited by 40

Aberrant Hippocampal Network Connectivity Is Associated With Neurocognitive Dysfunction in Patients With Moderate and Severe Obstructive Sleep Apnea

Zhou, L. Q., Liu, G., Luo, H., Li, H., Peng, Y., Zong, D., & Ouyang, R. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.580408 · Cited by 34

Structural and Functional Disruption of Salience Network in Distinguishing Subjective Cognitive Decline and Amnestic Mild Cognitive Impairment

Xue, C., Sun, H., Yue, Y., Wang, S., Qi, W., Hu, G., Ge, H., Yuan, Q., Rao, J., Tian, L., et al. (2021) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.1c00051 · Cited by 34

The hippocampus and spatial constraints on mental imagery

Bird, C. M., Bisby, J. A., & Burgess, N. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00142 · Cited by 41

The atypical antipsychotic risperidone reverses the recognition memory deficits induced by post-weaning social isolation in rats

McIntosh, A. L., Ballard, T. M., Steward, L. J., Moran, P. M., & Fone, K. C. F. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3011-2 · Cited by 35

Hippocampal signals for strong memory when associative memory is available and when it is not

Wais, P. E. (2009) · Hippocampus · doi:10.1002/hipo.20716 · Cited by 34

Using state-trace analysis to dissociate the functions of the human hippocampus and perirhinal cortex in recognition memory

Staresina, B. P., Fell, J., Dunn, J. C., Axmacher, N., & Henson, R. N. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1215710110 · Cited by 35

Understanding medial temporal activation in memory tasks: Evidence from fMRI of encoding and recognition in a case of transient global amnesia

Westmacott, R., Silver, F. L., & McAndrews, M. P. (2007) · Hippocampus · doi:10.1002/hipo.20397 · Cited by 34

Change in background context disrupts performance on visual paired comparison following hippocampal damage

Pascalis, O., Hunkin, N. M., Bachevalier, J., & Mayes, A. R. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.04.001 · Cited by 36

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Lux, V., Atucha, E., Kitsukawa, T., & Sauvage, M. M. (2016) · eLife · doi:10.7554/elife.11862 · Cited by 36

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Koganezawa, N., Gisetstad, R., Husby, E., Doan, T. P., & Witter, M. P. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0653-15.2015 · Cited by 36

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Simó, M., Rifà‐Ros, X., Vaquero, L., Ripollés, P., Cayuela, N., Jové, J., Navarro-Martín, A., Cardenal, F., Bruna, J., & Rodríguez‐Fornells, A. (2017) · Brain Imaging and Behavior · doi:10.1007/s11682-017-9697-8 · Cited by 37

Item and source memory for emotional associates is mediated by different retrieval processes

Ventura‐Bort, C., Dolcos, F., Wendt, J., Wirkner, J., Hamm, A. O., & Weymar, M. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.12.015 · Cited by 36

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Lamba, M. A. R. M. S. (2014) · IOSR Journal of Nursing and health Science · doi:10.9790/1959-03410104 · Cited by 33

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Borders, A. A., Aly, M., Parks, C. M., & Yonelinas, A. P. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.03.032 · Cited by 33

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within the medial temporal lobes

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